2-(5-nitro-1(3)H-imidazol-4-yl)-ethylamine | 92478-82-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-(5-nitro-1(3)H-imidazol-4-yl)-ethylamine
• 英文别名: 2-(5-Nitro-1h-imidazol-4-yl)-ethanamine；2-(5-nitro-1H-imidazol-4-yl)ethanamine
• CAS: 92478-82-5
• 化学式: C₅H₈N₄O₂
• 分子量: 156.144
• InChiKey: VGWDLSZZEJWDPM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  101
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-(N-{2-[(tert-Butoxycarbonyl)amino]ethyl}-N-(tert-butoxycarbonyl)aminomethyl)-4-methoxypyridine-6-carboxylic acid 、 2-(5-nitro-1(3)H-imidazol-4-yl)-ethylamine 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 生成 [2-(tert-Butoxycarbonyl-{4-methoxy-6-[2-(5-nitro-1H-imidazol-4-yl)-ethylcarbamoyl]-pyridin-2-ylmethyl}-amino)-ethyl]-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis and properties of prodrugs activated in hypoxia to give bleomycin analogues

  摘要：

  Prodrugs bioreductively activated to bleomycin analogues are reported. The production of hydroxyl radicals in the presence of Fe(II) and dioxygen by both the prodrugs and the activated products are determined and their in vitro cytotoxicity measured. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00467-3

文献信息

• Nagarajan,K. et al., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1977, vol. 15, p. 629 - 634
  作者：Nagarajan,K. et al.

  DOI：——

  日期：——
• Synthesis and properties of prodrugs activated in hypoxia to give bleomycin analogues
  作者：Jackie A. Highfield、Lina K. Mehta、John Parrick、Luis P. Candeias、Peter Wardman

  DOI：10.1016/s0960-894x(98)00467-3

  日期：1998.9

  Prodrugs bioreductively activated to bleomycin analogues are reported. The production of hydroxyl radicals in the presence of Fe(II) and dioxygen by both the prodrugs and the activated products are determined and their in vitro cytotoxicity measured. (C) 1998 Elsevier Science Ltd. All rights reserved.